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Lung virus titers were determined using a plaque assay [29], [30].
Using a plaque assay and evaluation of immediate-early 1 mRNA and protein expression, we found that mouse ES cells were resistant to murine CMV (MCMV) at the point of transcription.
Virus titer in the frozen culture supernatant was determined by using a plaque assay.
In addition, the mice tissues were collected for detecting live EV71 virus using a plaque assay.
Using a plaque assay, 23 BCC strains were tested for their sensitivity to KS10.
Virus isolation was attempted from pooled organs of RNA-positive birds by using a plaque assay on Vero cell culture.
Similar(51)
The EC50 value obtained for SPL7013 in our assay was similar to the value obtained using a plaque reduction assay for HSV [24].
Finally, the selected candidates were subjected to a biological validation assay to assess inhibition of Dengue virus propagation in mammalian host cells using a plaque formation assay.
The efficacy of silver nanoparticles and AgNO3 was determined using a plaque reduction assay similar to previously described methods [12].
Nanoparticles (10 80 nm, with or without polysaccharide coating), or silver nitrate (AgNO3) at concentrations of 100, 50, 25, and 12.5 μg/mL were evaluated for efficacy using a plaque reduction assay.
Virus blood titers were measured using a plaque forming assay as described [14].
More suggestions(15)
using a transwell assay
using a phototaxis assay
using a plaque reduction
using a fluctuation assay
using a radiolabel assay
using a plaque formation
using a chromogenic assay
using a TaqMan® assay
using a scratch assay
using a pcr assay
using a bioluminescence assay
using a luciferase assay
using a glucose assay
using a plate assay
using a qpcr assay
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